A leader in developing and providing healthcare is looking for a Process Validation Engineer in the Lexington, MA area. This is a 6-month CONTRACT position, with the possibility of extension. No per diem is available.
Responsibilities for the Process Engineer
- This role will be in the process transfer group supporting commercial, clinical, and technical processes. The individual will be expected to monitor and provide support for manufacturing purification operations.
- The individual will also be responsible for sampling and/or testing protocol authoring and review, as well as SOP and batch record review. Leadership and guidance of junior staff members in certain situations will also be expected.
- Responsibilities will include attending manufacturing morning meeting, daily production data trend review, event response and troubleshooting, batch review, deviation initiation support and manufacturing personnel training.
Requirements for the Process Engineer
- BS and 5+ years experience required. Biotech or pharmaceutical manufacturing background required.
<Benefits for the Process Engineer